Neck Musculoskeletal Symptoms Among Turkish Endodontists

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age25-65
SponsorAtlas University

About this trial

This observational study aims to evaluate the prevalence, severity, and characteristics of neck musculoskeletal symptoms among Turkish endodontists. Endodontists are exposed to prolonged static postures and repetitive movements during clinical procedures, which may increase the risk of neck-related disorders.

Participants will be asked to complete questionnaires regarding demographic characteristics, occupational factors, ergonomic conditions, and neck pain. In addition, physical assessments including cervical range of motion, muscle strength, endurance, posture, and proprioception will be performed using validated measurement tools.

The study also aims to identify factors associated with neck pain, such as working conditions, posture, and clinical experience. The findings may help improve preventive strategies, ergonomic recommendations, and rehabilitation approaches for dental professionals.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Aged 25 to 65 years

Actively practicing as an endodontist in Turkey in public institutions, university hospitals, or the private sector

Willing and able to provide informed consent

Endodontists with or without neck pain

Disqualifiers

History of cervical spine surgery within the last 3 months

History of cervical spine infection within the last 3 months (e.g., spondylodiscitis)

History of malignancy involving the cervical region

Spinal cord compression due to tumor or another cause

Trial population

The study population consists of actively practicing endodontists in Turkey, aged 25 to 65 years, working in public institutions, university hospitals, or the private sector. Participants with and without neck pain will be included to evaluate neck musculoskeletal symptoms, functional parameters, and associated occupational and ergonomic factors.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • No intervention (observational study)

    Other intervention

    This is an observational study with no therapeutic or experimental intervention. Participants will undergo questionnaire-based evaluations and physical assessments including cervical range of motion, muscle strength, endurance, posture, and proprioception measurements.

Treatment groups

120 Participants
are divided into 1 treatment group
Group A: Turkish Endodontists1 intervention

Trial outcomes

Primary outcomes

1

Prevalence and Severity of Neck Pain

Neck pain will be assessed using a self-reported questionnaire evaluating the presence, frequency, duration, and intensity of pain. Pain intensity will be measured using a numeric rating scale (0-10), where higher scores indicate greater pain severity.

Time frame
Baseline

Secondary outcomes

1

Neck Disability Index (NDI) Score

Functional disability related to neck pain will be assessed using the Neck Disability Index (NDI). The NDI consists of 10 items evaluating daily activities, each scored from 0 to 5. Total scores range from 0 to 50, with higher scores indicating greater disability.

Time frame
Baseline
2

Cervical Range of Motion

Cervical flexion, extension, lateral flexion, and rotation will be measured using the MicroFET 3 digital inclinometer. Range of motion values will be recorded in degrees for each movement direction.

Time frame
Baseline
3

Cervical Isometric Muscle Strength

Maximal isometric strength of cervical flexor, extensor, and lateral flexor muscles will be measured using the MicroFET 3 handheld dynamometer. Measurements will be performed in standardized positions and recorded.

Time frame
Baseline
4

Deep Cervical Flexor Muscle Endurance

Endurance of deep cervical flexor muscles will be assessed using the craniocervical flexion test with a pressure biofeedback unit. Performance will be recorded based on the ability to maintain target pressure levels.

Time frame
Baseline

Other outcomes

Sponsors and contacts

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